Busch Lab

ZMP

si:dkeyp-117h8.2

Ensembl ID:
ENSDARG00000011602
ZFIN ID:
ZDB-GENE-041210-321
Description:
Uncharacterized protein KIAA1211 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q5RG44]
Human Orthologue:
KIAA1211
Human Description:
KIAA1211 [Source:HGNC Symbol;Acc:29219]
Mouse Orthologue:
C530008M17Rik
Mouse Description:
RIKEN cDNA C530008M17 gene Gene [Source:MGI Symbol;Acc:MGI:2444817]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa43443 Nonsense Mutation detected in F1 DNA Not yet available
sa39278 Nonsense Mutation detected in F1 DNA Not yet available
sa1805 Splice Site F2 line generated Not yet available

Mutation Details

Allele Name:
sa43443
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000007754 Nonsense 172 1079 4 7
ENSDART00000146711 Nonsense 258 1165 5 8

The following transcripts of ENSDARG00000011602 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 25696505)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 25767808
GRCz11 20 25666898
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAAGTGTTTGATTCATCAAGAGAGGATTATGGTATTATCCATGGAAGT[A/T]AAGAAGATTATGAACCTACTGAAAAATCACAGAGGCAACGATTTCATGAG
Long Flanking Sequence:
ATGTCCTGCGCGAGTTCTCTTCAGGGTTTAAGGTTCAATGTTTAAATAAAAAAAGCTTGGAAATTTAGTTTAAACAGGAATAGCAACAAACAGTGTAGGCTTCTGGTCCCACATGCACTGACAAGCTGCACACGTAACTTTTTAGTTTTCACATGAAAGAGTCCATACCCTGAGTGCTCAGTGATGAGATATTGCATGGGCATTCATTCTATACATGCACAGGGCCCAATCAGAGAGTAATTAAAGGAATGAGAAAAACACAATTTTAATAAGTGTATTGAACCATGGAGTTCATACCGAACAGTTTATTATTATATTGAATATTGTGACATCCCTACTGTGAACTATAACTCAAAAGTATTAGGGTTTTAAGTTCTGTAACTTTGAATATATTTCAGGAGTTTCATGAAGATGATTTCTCTGAAATTCAAGAAGAATTTGAAAAGGATGAGGAAGTGTTTGATTCATCAAGAGAGGATTATGGTATTATCCATGGAAGT[A/T]AAGAAGATTATGAACCTACTGAAAAATCACAGAGGCAACGATTTCATGAGGAAGAGAAAGAACACCTTGAGATAAAGAAAAGAGAACAAGAGGAAGAGAGAAAGATGGAAAAACACCGGAGGATGATTGAGGAGCAGAGGTTAGAAGAAGAGAAGCGACGCAGACAGGAAGAGGAAAGGCTGCAAAAAGTGGAAGAGGAGAGGAAGCAACGAGAGGAAGAAGAGAGGAAAAAAAGGGAAGAGGAGGAAAGGAGGAGAGAAGAAGAAGAGCGAAGATTACGACATGAGGAAGAGCGAAAGAGACAAGAGGAGGAGGAAAGAATGAAGAAAGAAGAAGAAGAAAGAAAAAGAGCAGAAGAGGAAAGAAGGCAACAAGAACTTTTGGCAGAGCGTCTTCGTCTGGAAGAGGAAAGAAAAAGAGAACAGGAAGAGAGAAGGAGAAAAGAGGAGGAGGAGGCAGAGAAACGCAGGATTCAAGAGTTACAAGAGAAAAGGCTGAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39278
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000007754 Nonsense 201 1079 4 7
ENSDART00000146711 Nonsense 287 1165 5 8

The following transcripts of ENSDARG00000011602 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 25696418)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 25767721
GRCz11 20 25666811
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACGATTTCATGAGGAAGAGAAAGAACACCTTGAGATAAAGAAAAGAGAA[C/T]AAGAGGAAGAGAGAAAGATGGAAAAACACCGGAGGATGATTGAGGAGCAG
Long Flanking Sequence:
AAACAGTGTAGGCTTCTGGTCCCACATGCACTGACAAGCTGCACACGTAACTTTTTAGTTTTCACATGAAAGAGTCCATACCCTGAGTGCTCAGTGATGAGATATTGCATGGGCATTCATTCTATACATGCACAGGGCCCAATCAGAGAGTAATTAAAGGAATGAGAAAAACACAATTTTAATAAGTGTATTGAACCATGGAGTTCATACCGAACAGTTTATTATTATATTGAATATTGTGACATCCCTACTGTGAACTATAACTCAAAAGTATTAGGGTTTTAAGTTCTGTAACTTTGAATATATTTCAGGAGTTTCATGAAGATGATTTCTCTGAAATTCAAGAAGAATTTGAAAAGGATGAGGAAGTGTTTGATTCATCAAGAGAGGATTATGGTATTATCCATGGAAGTAAAGAAGATTATGAACCTACTGAAAAATCACAGAGGCAACGATTTCATGAGGAAGAGAAAGAACACCTTGAGATAAAGAAAAGAGAA[C/T]AAGAGGAAGAGAGAAAGATGGAAAAACACCGGAGGATGATTGAGGAGCAGAGGTTAGAAGAAGAGAAGCGACGCAGACAGGAAGAGGAAAGGCTGCAAAAAGTGGAAGAGGAGAGGAAGCAACGAGAGGAAGAAGAGAGGAAAAAAAGGGAAGAGGAGGAAAGGAGGAGAGAAGAAGAAGAGCGAAGATTACGACATGAGGAAGAGCGAAAGAGACAAGAGGAGGAGGAAAGAATGAAGAAAGAAGAAGAAGAAAGAAAAAGAGCAGAAGAGGAAAGAAGGCAACAAGAACTTTTGGCAGAGCGTCTTCGTCTGGAAGAGGAAAGAAAAAGAGAACAGGAAGAGAGAAGGAGAAAAGAGGAGGAGGAGGCAGAGAAACGCAGGATTCAAGAGTTACAAGAGAAAAGGCTGAGAGAGGAAGAACATCGCATTCGTGAAGAAGAAAGATGTCGACAAGAGGAAGCAGAGAGAAAAAGACTAGAGGAAGAGGAAAGAAAGAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1805
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000007754 Splice Site None 1079 None 7
ENSDART00000146711 Splice Site None 1165 None 8

The following transcripts of ENSDARG00000011602 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 25693207)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 25764510
GRCz11 20 25663600
KASP Assay ID:
554-1797.1 (used for ordering genotyping assays)
KASP Sequence:
CTTAGTCTTTATTGCCAATTTAACAGACCTTCTGCATTTCTTCTCCTTAT[C/T]AGAAAAACCATCTCTGCAGGCCAGGCATTCTCTGGACAGCTCACGATCAC
Long Flanking Sequence:
ATATCGTTTTAGTCGTTTGATATGCTGTGACGCAGTCAAATATTTCACTGAACAGATCAGCCACTTTTGACGCTCATAAACAATCATAAAGTCTTCGTGCTGCAGGAATTAGGAGGTTTGCTAAAGGTGCAGCTGTCATGCAGTGAGGGGTTTGTGTCTTTAATAAACTACAGCAGTTTGCGTTCATAGAACAGTAAGAATGATTAATTAATCCATATGAAACAGTATGTTAAAAGTCCATCTCGCCTTCAGTTTCGGGCTCAGGCATGCTTTGCACTCACACTACAAGCGTACCACACCCAAGTAAACCGCGCTCAGGCACACCTCTTCCAACCGGGCCAGGGCCAGCCAAGTGAACCGTGCCTGAGCCCGATTCAGAGCACTCACACTTATCAAACGATCCAGGACACGGGCATGGGCACGGTTCAGATAGCATAGTGTGAGTACACCCTTAGTCTTTATTGCCAATTTAACAGACCTTCTGCATTTCTTCTCCTTAT[C/T]AGAAAAACCATCTCTGCAGGCCAGGCATTCTCTGGACAGCTCACGATCACAGGACAAAGAGACAGGACCACTTTGGATCACTCTGGCACTGCAAAAACAGAAAGGCTTTAGGGAACAGCAGCAAAACCGAGAGGAAAGGAGGAACCAGAGAGAGGCTAAACTGGCTGAGAAACAAGCTAGGGACAGAGAAAGTGTATGTATTAACAAAAGCACTGTCCCATAGTGTATTATCATTCATTAGCTACCCTGTTAGTACTGTATACATAATTGTAATATTGCTTTGTGAATTTATAGCAAAAGTTCTCACTCTTGTTTCTGGAAGTCAGTTGCTAGTTCCACCTTCTTGAGCTTTGATAGATGCAAACTATTTTGTCACATGAAAACTAGTGAGGGCGCAGTATAATATTATAAAAAATGAACTCCTCTGTATTAATAGAATTTGGTGTTGTTGTTTCTTTATCTGAAAGGCTGGAAGCAGTCCCACTGAGGATAAAGGCAAT
Associated Phenotype:
Not determined